Taiwan FDA registration 5f7daa8c361f171529629a39ff1945b0

"Lianghong" corrective lenses (unsterilized)

TW: "良宏" 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·HANMI SWISS OPTICAL CO., LTD.·Registered May 07, 2012 – May 07, 2017Cancelled
Registration details
Analysis ID
5f7daa8c361f171529629a39ff1945b0
Customs Code
DHA04401166606
Company information
Manufacturer Country
Korea, Republic of
Authorized Representative
Lianghong Optoelectronics Co., Ltd
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.5844 corrective lenses
Import Information
import
Dates and status
Registration Date
May 07, 2012
Expiry Date
May 07, 2017
Cancellation Date
Jan 06, 2020
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for "Lianghong" corrective lenses (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5f7daa8c361f171529629a39ff1945b0 and manufactured by HANMI SWISS OPTICAL CO., LTD.. The authorized representative in Taiwan is Lianghong Optoelectronics Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including DANYANG HENRY OPTICAL CO., LTD, Lianghong Optoelectronics Co., Ltd, and 2 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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